Patent classifications
B01L3/502746
Microfluidic Device for the Generation of Combinatorial Samples
The present disclosure relates to a microfluidic device and a method allowing the generating and screening of combinatorial samples. A microfluidic device for producing droplets of at least one sample into an immiscible phase is provided, the device comprising a droplet maker connecting an immiscible phase channel and a sample channel having at least one sample inlet connected to at least one sample inlet channel injecting the at least one sample into the sample channel, wherein the injection of the at least one sample is controlled by at least one sample valve, so that the at least one sample flows either towards a sample waste outlet or into the at least one sample inlet channel, wherein different sample inlet channel of the at least one sample inlet channel have the same hydrodynamic resistance resulting from the length, height and width of each sample inlet channel upstream of the droplet maker.
MICROFLUIDIC ANALYSIS DEVICE AND METHOD
The present invention relates to a microfluidic analysis device (1) including: a substrate (20) wherein a separation channel (10) is arranged, in which an electrolyte flows, a portion of the separation channel (10) being covered with a polarisable surface (11); two longitudinal field electrodes (8a, 8b) arranged on either side of the separation channel (10); at least one control electrode (6a, 6b) positioned in the separation channel (10), the control electrode (6a, 6b) being suitable for polarising the polarisable surface (11) so as to control the speed of the electro-osmotic flow in the separation channel (10); the microfluidic analysis device (1) being characterised in that the polarisable surface (11) includes an insulating sub-layer (12) made of amorphous silicon carbide (SiC) and an upper polarisable layer (13) in direct contact with the electrolyte, the control electrodes (6a, 6b) being positioned between the insulating sub-layer (12) and the upper polarisable layer (13).
CHEMICAL REACTORS
A chemical reactor is implemented on a substrate. The chemical reactor has multiple ducts for transporting a fluid and/or gas during use of the chemical reactor, in which the ducts optionally include pillar structures and at least one connection duct connected between two of the multiple ducts for transporting the fluid and/or gas from one duct to another. In the connection duct, a series of individual pillar structures are positioned behind each other in the longitudinal direction of the connection duct.
SYSTEM AND METHOD FOR DEFORMING PARTICLES
Embodiments of a system and method for deforming a can include a substrate including an inlet module and an outlet module; a fluidic pathway coupled to the inlet module and the outlet module, and including a sample branch operable to transmit the sample fluid; one or more sheath fluid branches flanking the sample branch and operable to transmit sheath having a sheath fluid viscosity higher than a sample fluid viscosity of the sample fluid; a delivery region initiating at a junction between the sample branch and the one or more sheath fluid branches, and operable to transmit a co-flow comprising the sample fluid and the sheath fluid; and a deformation region located downstream of the delivery region and operable to deform the one or more particles of the sample fluid based upon a reduced velocity of the sheath fluid with respect to the sample fluid in the co-flow.
Microfluid device and method of producing diffusively built gradients
A microfluid device for producing diffusively built gradients comprising a bottom plate and a cover plate, wherein the cover plate has recesses and is connected to the bottom plate in a liquid-tight manner so that the recesses form at least two reservoirs and one observation chamber, which connects the reservoir, a reservoir can be filled particularly through an inlet/outlet through the cover plate, and the cross-sectional surface of the observation chamber is at least 5 times, preferably at least 200 times smaller at the aperture of the observation chamber into one of the reservoirs than the maximum cross-sectional surface of the reservoir in parallel to this cross-sectional surface of the observation chamber.
DETECTION CHIP AND METHOD OF MANUFACTURING DETECTION CHIP
A detection chip and a method of manufacturing a detection chip are disclosed. The detection chip includes a first substrate, a plurality of detection units, and at least one diversion dam. The plurality of detection units are located on the first substrate, the diversion dam is located on the first substrate, and the diversion dam extends along a first path and is located between adjacent detection units.
DEVICE FOR SEPARATING BUBBLES FROM A FLUID
The present invention relates to a device and a method for separating bubbles from a fluid comprising a chamber through which a fluid can pass. According to the invention the device is characterized in that the inner chamber wall has a geometry that generates within said chamber a continuous flow and at least one area with a discontinuous flow which has a low flow velocity so that bubbles remain at the inner chamber wall in said area and thus are separated from the fluid flowing out from the chamber.
METHODS, DEVICES, AND SYSTEMS FOR MICROFLUIDIC STRESS EMULATION
Provided herein is technology relating to microfluidic devices and particularly, but not exclusively, to devices, methods, systems, and kits for imparting stresses on a fluid flowing through a microfluidic device that is designed to mimic a stress profile of a macrofluidic device or pathology.
SYSTEMS AND METHODS FOR INTEGRATION OF MICROFLUIDIC TEAR COLLECTION AND LATERAL FLOW ANALYSIS OF ANALYTES OF INTEREST
Systems, methods, and devices for analyzing small volumes of fluidic samples, as a non-limiting example, less than twenty microliters are provided. The devices are configured to make a first sample reading, for example, measure an energy property of the fluid sample, for example, osmolality, make a second sample reading, for example, detecting the presence or concentration of one or more analytes in the fluid sample, or make both the first sample reading and the second sample reading, for example, measuring the energy property of the fluid sample as well as detecting the presence or concentration of one or more analytes in the fluid sample.
METHODS AND DEVICES FOR MULTI-STEP CELL PURIFICATION AND CONCENTRATION
Described herein are microfluidic devices and methods that can separate and concentrate particles in a sample.